Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.
Primary Purpose
Inguinal Hernia
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ultra sound guided nerve block
Usual infiltration
Sponsored by
About this trial
This is an interventional supportive care trial for Inguinal Hernia
Eligibility Criteria
Inclusion criteria:
- Patients who underwent elective inguinal hernia repair (will consider the hernia size).
- Age from 18-70. (70 with no other comorbiditeis)
- Their ASA score 1,2 or 3 (American Society of Anesthesia)
- General Anesthesia.
- Open inguinal hernia repair.
Exclusion criteria:
- All emergency inguinal hernia repair and recurrent hernia.
- Children and pregnant women.
- Patients having regional anesthesia. (Spinal/Local).
- Laparoscopic inguinal hernia.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
The experimental group will receive US guided nerve block
The control group will receive usual infiltration
Arm Description
The experimental group will receive US guided nerve block by lidocaine before open inguinal hernia repair.
The control group will receive usual infiltration by lidocaine before open inguinal hernia repair.
Outcomes
Primary Outcome Measures
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Assessment of pain scale post operative, lower score mean a better outcome.
Assessment of early mobilisation.
When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
Assessment of early mobilisation.
When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
Assessment of early mobilisation.
When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
Retain to driving (how many days between surgery and patient back to dive)
When the patient back to drive his car? assessed by monitoring the patients postoperative and record when he started to drive the car again.
Retain to work (how many days between surgery and patient back to his work)
When the patient back to his work or usual activity? assessed by monitoring the patients postoperative and record when he started to work again.
Length of hospital stay (in days).
Length of hospital stay post open inguinal hernia repair ( how many days patient spend in the hospital postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Frequency of analgesia consumption postoperative.
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Secondary Outcome Measures
Full Information
NCT ID
NCT04792164
First Posted
February 9, 2021
Last Updated
October 31, 2021
Sponsor
Imam Abdulrahman Bin Faisal University
1. Study Identification
Unique Protocol Identification Number
NCT04792164
Brief Title
Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.
Official Title
Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair: Randomised Control Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2021 (Anticipated)
Primary Completion Date
December 29, 2022 (Anticipated)
Study Completion Date
June 29, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Imam Abdulrahman Bin Faisal University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
A hernia occurs when an organ 'like intestines' or fatty tissue protrude through a weak point in muscle or connective tissue and one of the most common types of hernia is inguinal. Inguinal hernia defined as a bulge in the inguinal region or scrotum, may be accompanied by dull or burning pain, which worsens by exercise or cough. There are 2 types of inguinal hernia: direct and indirect. Direct inguinal hernia occurs because of a defect or weakness in the transversalis fascia area of the Hesselbach triangle. On the other hand, the indirect inguinal hernia which is the most common inguinal hernia follows the tract of inguinal canal and result from a persistent processus vaginalis.
Immediate pain after inguinal herniorrhaphy delays the ambulation which leads to delay in the hospital discharge. Besides that, is the chronic pain that affect 50% of patients which is an important issue that needs to be dealt with.
Our aim of this study, is to compare between postoperative period in the patients who received US guided nerve block and in patients who received infiltration only before open inguinal hernia repair, and to show that pre-emptive local anaesthesia will result in better pain control, less postoperative complication, earlier mobilisation, earlier recovery and less analgesia consumption by patients.
Detailed Description
In this study our aim in detail is to:
Asses the outcomes (early postoperative pain management in day case "day 1,2,3, 30 and 3 month and 6 month" , length of hospital stay, analgesia consumption، recovery to work, driving and usual activity) of the US guided nerve block in patients who underwent inguinal hernia repair comparing to patient who received only skin infiltration.
Evaluate the advantages of the US guided nerve block in postoperative inguinal hernia repair patients.
Demonstrate its compatibly as a one day procedure (less length of hospital stay), with earlier return to work and driving and recovery in general.
Compare our result with other international studies result.
Study in details:
it is Randomised Control Trial, Double blinded (patients and recruiter), study will be conducted in King Fahd University Hospital, Khobar, Eastern Province, Saudi Arabia. It contains 2 Arms ,Two Parallel groups. The experimental group will receive US guided nerve block and the control group will receive usual infiltration. Lidocaine+ Marcaine will be used in both group with same concentration (1%+.25%). The random allocation will be done using simple random allocation with a help of the following software (random.org).
Will compare the two groups regarding, a questionary with visual analogue will be distributed and data will be collected by recruiters regarding pain scale, length of hospital stay, return to work, return to driving and usual activity, and analgesia consumption post operative, all in day 1,2,3,4,30,3 month and 6 month post operatives (details in outcome section).
We are expecting to have a reduction in pain score from severe to moderate, about 20% in experimental group, and reducing the length of hospital stay from 1-2 days to one day procedure. And reduction in consumption of Analgesia postoperative.
our sample size will be 134 with a power of 80% and an effect size of 0.5, will include all patients who will have inguinal hernia repair and meet our inclusion criteria, in period of 12-18 months starting after obtaining of IRB approval.
Inclusion criteria:
Patients who underwent elective inguinal hernia repair (will consider the hernia size).
Age from 18-70.
Their ASA score 1,2 or 3 (American Society of Anesthesia)
Operation under general anaesthesia.
Open inguinal hernia repair.
Exclusion criteria:
All emergency inguinal hernia repair and recurrent hernia.
Children and pregnant women.
Patients having regional anaesthesia. (Spinal/Local).
Laparoscopic inguinal hernia.
Data Management and analysis plan:
SPSS latest version will be used for data analysis.
Summary statistic will be obtained as frequency, and percentage for qualitative data, and means, medians and standard deviations from continuous variables.
Analysis will be done by epidemiologist and biostatistician.
Ethical Considerations:
Our study does not have any physical, psychological, social, legal, economic risk.
The study will be reviewed by IRB, ethics committee; then the approval will be obtained.
Written approval will be obtained from the patients prior to the procedure.
Preemptive analgesia and infiltration are usually used in our practice and aim to compare.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inguinal Hernia
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2 Arms
Arm1) The experimental group will receive US guided nerve block by Lidocaine+Marcaine concentration (1%+.25%).
Arm2) The control group will receive usual infiltration by Lidocaine+Marcaine concentration (1%+.25%).
Masking
ParticipantOutcomes Assessor
Masking Description
Double blinded ( Patient and researcher recruiter)
Allocation
Randomized
Enrollment
136 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
The experimental group will receive US guided nerve block
Arm Type
Experimental
Arm Description
The experimental group will receive US guided nerve block by lidocaine before open inguinal hernia repair.
Arm Title
The control group will receive usual infiltration
Arm Type
Other
Arm Description
The control group will receive usual infiltration by lidocaine before open inguinal hernia repair.
Intervention Type
Procedure
Intervention Name(s)
Ultra sound guided nerve block
Intervention Description
Ultra sound guided nerve block by lidocaine before open inguinal hernia repair.
Intervention Type
Procedure
Intervention Name(s)
Usual infiltration
Intervention Description
Usual infiltration by lidocaine before open inguinal hernia repair.
Primary Outcome Measure Information:
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
Day 1 postoperative.
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
Day 2 postoperative.
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
Day 3 postoperative.
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
Day 4 postoperative.
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
Day 30 postoperative.
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
3 month postoperative for chronic pain.
Title
Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
Description
Assessment of pain scale post operative, lower score mean a better outcome.
Time Frame
6 month postoperative for chronic pain.
Title
Assessment of early mobilisation.
Description
When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
Time Frame
Day 1 postoperative period.
Title
Assessment of early mobilisation.
Description
When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
Time Frame
Day 2 postoperative period.
Title
Assessment of early mobilisation.
Description
When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
Time Frame
Day 3 postoperative period.
Title
Retain to driving (how many days between surgery and patient back to dive)
Description
When the patient back to drive his car? assessed by monitoring the patients postoperative and record when he started to drive the car again.
Time Frame
Postoperative period up to 8 weeks.
Title
Retain to work (how many days between surgery and patient back to his work)
Description
When the patient back to his work or usual activity? assessed by monitoring the patients postoperative and record when he started to work again.
Time Frame
Postoperative period up to 8 weeks.
Title
Length of hospital stay (in days).
Description
Length of hospital stay post open inguinal hernia repair ( how many days patient spend in the hospital postoperative).
Time Frame
immediately after the surgery until patient discharged.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 1 postoperative.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 2 postoperative.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 3 postoperative.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 4 postoperative.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 5 postoperative.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 6 postoperative.
Title
Frequency of analgesia consumption postoperative.
Description
Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
Time Frame
Day 7 postoperative.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Patients who underwent elective inguinal hernia repair (will consider the hernia size).
Age from 18-70. (70 with no other comorbiditeis)
Their ASA score 1,2 or 3 (American Society of Anesthesia)
General Anesthesia.
Open inguinal hernia repair.
Exclusion criteria:
All emergency inguinal hernia repair and recurrent hernia.
Children and pregnant women.
Patients having regional anesthesia. (Spinal/Local).
Laparoscopic inguinal hernia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nasser M Amer
Phone
00966 53 865 9290
Email
nmamer@iau.edu.sa
12. IPD Sharing Statement
Learn more about this trial
Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.
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